Canonical Allele Identifier: CA2266876322

Gene: NOG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56594709C= , CM000679.2:g.56594709C=	GRCh38
NC_000017.10:g.54672070C= , CM000679.1:g.54672070C=	GRCh37
NC_000017.9:g.52027069C=	NCBI36
NG_011958.1:g.6011C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000332822.6:c.486C= MANE Select	ENSP00000328181.4:p.Asn162=
ENST00000332822.4:c.486C=	ENSP00000328181.4:p.Asn162=
NM_005450.4:c.486C=	NP_005441.1:p.Asn162=
NM_005450.6:c.486C= MANE Select	NP_005441.1:p.Asn162=